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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K071107
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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CR-FLEX GSF PRECOAT SZ C-L® CR-FLEX GSF PRECOAT SZ C-R® CR-FLEX GSF PRECOAT SZ D-L® CR-FLEX GSF P... 2 03/14/2018 Zimmer Biomet, Inc.
CR-FLEX GSF PCT SZ C-R MINUS® CR-FLEX GSF PCT SZ D-L MINUS® CR-FLEX GSF PCT SZ D-R MINUS® CR-FLEX... 2 03/14/2018 Zimmer Biomet, Inc.
GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM FEMORAL COMPONENT® N-K FLX GSM POR FEM SZ 2 RT N-K FL... 2 03/14/2018 Zimmer Biomet, Inc.
GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENT NONPOROUS®... 2 03/14/2018 Zimmer Biomet, Inc.
CR Flex GSF Precoat Fem Natural Knee GSF NP Flex Natural Knee GSF POR Flex Natural Knee GSM NP Fl... 2 02/22/2016 Zimmer Biomet, Inc.
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